CA1113487A - Anthranilates de carboxamides oxyalkyles - Google Patents
Anthranilates de carboxamides oxyalkylesInfo
- Publication number
- CA1113487A CA1113487A CA318,136A CA318136A CA1113487A CA 1113487 A CA1113487 A CA 1113487A CA 318136 A CA318136 A CA 318136A CA 1113487 A CA1113487 A CA 1113487A
- Authority
- CA
- Canada
- Prior art keywords
- bis
- formula
- acid diamide
- compound
- anthranilates
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical class NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 title claims abstract description 10
- 150000003857 carboxamides Chemical class 0.000 title abstract description 3
- 150000001875 compounds Chemical class 0.000 claims abstract description 28
- VYFOAVADNIHPTR-UHFFFAOYSA-N isatoic anhydride Chemical compound NC1=CC=CC=C1CO VYFOAVADNIHPTR-UHFFFAOYSA-N 0.000 claims abstract description 24
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 19
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 9
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims abstract description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 4
- 239000001257 hydrogen Substances 0.000 claims abstract 4
- 150000001990 dicarboxylic acid derivatives Chemical class 0.000 claims abstract 2
- 238000000034 method Methods 0.000 claims description 9
- 238000002360 preparation method Methods 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 2
- 235000013350 formula milk Nutrition 0.000 claims 5
- BLQBQQSFAWHFGD-UHFFFAOYSA-N 2-[2-(anthracene-1-carbonyloxy)ethyl-[2-[bis[2-(anthracene-1-carbonyloxy)ethyl]amino]-2-oxoacetyl]amino]ethyl anthracene-1-carboxylate Chemical compound C1(=CC=CC2=CC3=CC=CC=C3C=C12)C(=O)OCCN(C(C(=O)N(CCOC(=O)C1=CC=CC2=CC3=CC=CC=C3C=C12)CCOC(=O)C1=CC=CC2=CC3=CC=CC=C3C=C12)=O)CCOC(=O)C1=CC=CC2=CC3=CC=CC=C3C=C12 BLQBQQSFAWHFGD-UHFFFAOYSA-N 0.000 claims 1
- QGCCHFKVIRKONV-UHFFFAOYSA-N 2-[[10-[2-(anthracene-1-carbonyloxy)ethylamino]-10-oxodecanoyl]amino]ethyl anthracene-1-carboxylate Chemical compound C1(=CC=CC2=CC3=CC=CC=C3C=C12)C(=O)OCCNC(CCCCCCCCC(=O)NCCOC(=O)C1=CC=CC2=CC3=CC=CC=C3C=C12)=O QGCCHFKVIRKONV-UHFFFAOYSA-N 0.000 claims 1
- OOGGGAMKHHHDPY-UHFFFAOYSA-N 2-[[2-[2-(anthracene-1-carbonyloxy)ethylamino]-2-oxoacetyl]amino]ethyl anthracene-1-carboxylate Chemical compound C1(=CC=CC2=CC3=CC=CC=C3C=C12)C(=O)OCCNC(C(=O)NCCOC(=O)C1=CC=CC2=CC3=CC=CC=C3C=C12)=O OOGGGAMKHHHDPY-UHFFFAOYSA-N 0.000 claims 1
- CXISRIJHIISQMV-UHFFFAOYSA-N 2-[[4-[2-(anthracene-1-carbonyloxy)ethylamino]-4-oxobutanoyl]amino]ethyl anthracene-1-carboxylate Chemical compound C1(=CC=CC2=CC3=CC=CC=C3C=C12)C(=O)OCCNC(CCC(=O)NCCOC(=O)C1=CC=CC2=CC3=CC=CC=C3C=C12)=O CXISRIJHIISQMV-UHFFFAOYSA-N 0.000 claims 1
- AMVCFEWWGVCBTG-UHFFFAOYSA-N 2-[[4-[2-(anthracene-1-carbonyloxy)ethylcarbamoyl]benzoyl]amino]ethyl anthracene-1-carboxylate Chemical compound C1(=CC=CC2=CC3=CC=CC=C3C=C12)C(=O)OCCNC(C1=CC=C(C(=O)NCCOC(=O)C2=CC=CC3=CC4=CC=CC=C4C=C23)C=C1)=O AMVCFEWWGVCBTG-UHFFFAOYSA-N 0.000 claims 1
- NNJXAKRBGSNPGD-UHFFFAOYSA-N N,N'-bis(2-anthracen-1-yl-2-oxoethoxy)hexanediamide Chemical compound C1(=CC=CC2=CC3=CC=CC=C3C=C12)C(=O)CONC(CCCCC(=O)NOCC(=O)C1=CC=CC2=CC3=CC=CC=C3C=C12)=O NNJXAKRBGSNPGD-UHFFFAOYSA-N 0.000 claims 1
- 239000003431 cross linking reagent Substances 0.000 abstract description 6
- 229920005989 resin Polymers 0.000 abstract description 6
- 239000011347 resin Substances 0.000 abstract description 6
- 239000003054 catalyst Substances 0.000 abstract description 5
- 239000004814 polyurethane Substances 0.000 abstract description 5
- 229920002396 Polyurea Polymers 0.000 abstract description 4
- 239000003795 chemical substances by application Substances 0.000 abstract description 4
- 229920002635 polyurethane Polymers 0.000 abstract description 4
- 238000004519 manufacturing process Methods 0.000 abstract description 3
- 229920000647 polyepoxide Polymers 0.000 abstract description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 39
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 34
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 30
- 239000000047 product Substances 0.000 description 27
- 239000000203 mixture Substances 0.000 description 20
- 235000011121 sodium hydroxide Nutrition 0.000 description 13
- 229940083608 sodium hydroxide Drugs 0.000 description 13
- 239000013078 crystal Substances 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 11
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- -1 oxyalkylated dicarboxylic acid diamides Chemical class 0.000 description 10
- 239000000843 powder Substances 0.000 description 10
- 238000002844 melting Methods 0.000 description 9
- 230000008018 melting Effects 0.000 description 9
- 239000000126 substance Substances 0.000 description 8
- IBOFVQJTBBUKMU-UHFFFAOYSA-N 4,4'-methylene-bis-(2-chloroaniline) Chemical compound C1=C(Cl)C(N)=CC=C1CC1=CC=C(N)C(Cl)=C1 IBOFVQJTBBUKMU-UHFFFAOYSA-N 0.000 description 7
- 238000001228 spectrum Methods 0.000 description 7
- 238000005160 1H NMR spectroscopy Methods 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 241001112258 Moca Species 0.000 description 5
- 238000000746 purification Methods 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- 238000007792 addition Methods 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- 238000009838 combustion analysis Methods 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000004411 aluminium Substances 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 235000010210 aluminium Nutrition 0.000 description 3
- 150000002009 diols Chemical class 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000000875 corresponding effect Effects 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- 230000008030 elimination Effects 0.000 description 2
- 238000003379 elimination reaction Methods 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000012452 mother liquor Substances 0.000 description 2
- PDECHAVKIJHTRQ-UHFFFAOYSA-N n,n'-bis(2-hydroxyethyl)butanediamide Chemical compound OCCNC(=O)CCC(=O)NCCO PDECHAVKIJHTRQ-UHFFFAOYSA-N 0.000 description 2
- AGSPVKCNWHGSQZ-UHFFFAOYSA-N n,n'-bis(2-hydroxyethyl)decanediamide Chemical compound OCCNC(=O)CCCCCCCCC(=O)NCCO AGSPVKCNWHGSQZ-UHFFFAOYSA-N 0.000 description 2
- OSGRUAAPIRXZTJ-UHFFFAOYSA-N n,n'-bis(2-hydroxyethyl)hexanediamide Chemical compound OCCNC(=O)CCCCC(=O)NCCO OSGRUAAPIRXZTJ-UHFFFAOYSA-N 0.000 description 2
- FPQJEXTVQZHURJ-UHFFFAOYSA-N n,n'-bis(2-hydroxyethyl)oxamide Chemical compound OCCNC(=O)C(=O)NCCO FPQJEXTVQZHURJ-UHFFFAOYSA-N 0.000 description 2
- 239000003791 organic solvent mixture Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 238000005809 transesterification reaction Methods 0.000 description 2
- ATIAIEWDRRJGSL-UHFFFAOYSA-N 1,3-bis(2-hydroxyethyl)-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(CCO)C(=O)N(CCO)C1=O ATIAIEWDRRJGSL-UHFFFAOYSA-N 0.000 description 1
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- KQIXMZWXFFHRAQ-UHFFFAOYSA-N 1-(2-hydroxybutylamino)butan-2-ol Chemical compound CCC(O)CNCC(O)CC KQIXMZWXFFHRAQ-UHFFFAOYSA-N 0.000 description 1
- VNXJRBGZIXAZRZ-UHFFFAOYSA-N 1-n,4-n-bis(2-hydroxyethyl)benzene-1,4-dicarboxamide Chemical compound OCCNC(=O)C1=CC=C(C(=O)NCCO)C=C1 VNXJRBGZIXAZRZ-UHFFFAOYSA-N 0.000 description 1
- BSESQBBHCKBEIW-UHFFFAOYSA-N 2-amino-4-[(3-amino-4-carboxyphenyl)methyl]benzoic acid Chemical class C1=C(C(O)=O)C(N)=CC(CC=2C=C(N)C(C(O)=O)=CC=2)=C1 BSESQBBHCKBEIW-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- SLAMLWHELXOEJZ-UHFFFAOYSA-N 2-nitrobenzoic acid Chemical compound OC(=O)C1=CC=CC=C1[N+]([O-])=O SLAMLWHELXOEJZ-UHFFFAOYSA-N 0.000 description 1
- BLFRQYKZFKYQLO-UHFFFAOYSA-N 4-aminobutan-1-ol Chemical compound NCCCCO BLFRQYKZFKYQLO-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 238000006418 Brown reaction Methods 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- WUGQZFFCHPXWKQ-UHFFFAOYSA-N Propanolamine Chemical compound NCCCO WUGQZFFCHPXWKQ-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000000010 aprotic solvent Substances 0.000 description 1
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 231100000315 carcinogenic Toxicity 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000000306 component Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 229940117389 dichlorobenzene Drugs 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- JXCHMDATRWUOAP-UHFFFAOYSA-N diisocyanatomethylbenzene Chemical compound O=C=NC(N=C=O)C1=CC=CC=C1 JXCHMDATRWUOAP-UHFFFAOYSA-N 0.000 description 1
- 229940113088 dimethylacetamide Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002118 epoxides Chemical class 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- VDCPMPXVRGYTQY-UHFFFAOYSA-N n,n,n',n'-tetrakis(2-hydroxyethyl)oxamide Chemical compound OCCN(CCO)C(=O)C(=O)N(CCO)CCO VDCPMPXVRGYTQY-UHFFFAOYSA-N 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229920001610 polycaprolactone Polymers 0.000 description 1
- 239000004632 polycaprolactone Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920003225 polyurethane elastomer Polymers 0.000 description 1
- 229920003226 polyurethane urea Polymers 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000000967 suction filtration Methods 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/50—Amines
- C08G59/54—Amino amides>
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/38—Low-molecular-weight compounds having heteroatoms other than oxygen
- C08G18/3819—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen
- C08G18/3823—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen containing -N-C=O groups
- C08G18/3825—Low-molecular-weight compounds having heteroatoms other than oxygen having nitrogen containing -N-C=O groups containing amide groups
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyurethanes Or Polyureas (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH15123/77 | 1977-12-09 | ||
| CH1512377 | 1977-12-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1113487A true CA1113487A (fr) | 1981-12-01 |
Family
ID=4406538
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA318,136A Expired CA1113487A (fr) | 1977-12-09 | 1978-12-07 | Anthranilates de carboxamides oxyalkyles |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US4174455A (fr) |
| JP (1) | JPS5492936A (fr) |
| AT (1) | AT361458B (fr) |
| CA (1) | CA1113487A (fr) |
| DE (1) | DE2852785A1 (fr) |
| FR (1) | FR2411173A1 (fr) |
| GB (1) | GB2010265A (fr) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4339383A (en) * | 1979-07-11 | 1982-07-13 | Ciba-Geigy Corporation | Imide containing stabilizers for chlorinated thermoplastics |
| US4328322A (en) * | 1979-12-03 | 1982-05-04 | Polaroid Corporation | Synthetic polymers by polyisocyanate polyaddition process |
| US4493909A (en) * | 1981-06-25 | 1985-01-15 | Bayer Aktiengesellschaft | Poly-N,N-hydroxyalkylamides of polybasic carboxylic acids and a process for the production thereof |
| US4822518A (en) * | 1987-12-11 | 1989-04-18 | Ashland Oil, Inc. | Convenient synthesis of polyamide polyol/urethane diol blends |
| DE4123543A1 (de) * | 1991-07-16 | 1993-01-21 | Albrecht Dipl Ing Muehlhaus | Vorrichtung zur magnetischen wasserbehandlung |
| CN1057540C (zh) * | 1995-09-26 | 2000-10-18 | 财团法人工业技术研究院 | 含酰胺键的聚氨酯制品 |
| EP0950923B1 (fr) * | 1997-11-05 | 2006-04-19 | Tokyo Ohka Kogyo Co., Ltd. | Composition de resine photosensible et plaque de resine flexographique |
| JP4873208B2 (ja) * | 2001-03-28 | 2012-02-08 | ナガセケムテックス株式会社 | 新規化合物ならびにそれを用いた吸水性樹脂用架橋剤および吸水性樹脂 |
| CN115785369B (zh) * | 2022-12-07 | 2025-12-23 | 西安交通大学 | 一种聚氨酯扩链剂与高强度聚氨酯 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3123631A (en) * | 1964-03-03 | Process for preparing esters of | ||
| GB808366A (en) * | 1955-07-29 | 1959-02-04 | Cellulose Sidac Soc Ind De | Film forming composition with plasticizer of terephthalamide derivatives |
| US3271440A (en) * | 1962-10-09 | 1966-09-06 | Gen Aniline & Film Corp | Amino-benzoic and amino-toluic acid diesters of polyhydric alkanols |
| FR1580319A (fr) * | 1968-06-21 | 1969-09-05 | ||
| DE2160590A1 (de) * | 1971-12-07 | 1973-06-14 | Bayer Ag | Neue aromatische polyamine, ein verfahren zu ihrer herstellung und ihre verwendung zur herstellung von polyurethanen |
| US4129741A (en) * | 1975-10-27 | 1978-12-12 | Lim-Holding, S.A. | Novel polyethers having terminal amino groups, a process for their production and their application |
-
1978
- 1978-12-04 US US05/966,417 patent/US4174455A/en not_active Expired - Lifetime
- 1978-12-06 DE DE19782852785 patent/DE2852785A1/de not_active Withdrawn
- 1978-12-07 AT AT875578A patent/AT361458B/de not_active IP Right Cessation
- 1978-12-07 CA CA318,136A patent/CA1113487A/fr not_active Expired
- 1978-12-08 JP JP15260378A patent/JPS5492936A/ja active Pending
- 1978-12-08 FR FR7834597A patent/FR2411173A1/fr active Granted
- 1978-12-11 GB GB7847933A patent/GB2010265A/en not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| AT361458B (de) | 1981-03-10 |
| FR2411173B1 (fr) | 1982-02-05 |
| JPS5492936A (en) | 1979-07-23 |
| ATA875578A (de) | 1980-08-15 |
| DE2852785A1 (de) | 1979-06-13 |
| GB2010265A (en) | 1979-06-27 |
| FR2411173A1 (fr) | 1979-07-06 |
| US4174455A (en) | 1979-11-13 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKEX | Expiry |